Отправить статью по E-mail Cyclic Amidoalkylation of Hydrophosphorylic Compounds. Synthesis of Proline Analogs
- Авторы: Vinyukov A.1, Dmitriev M.1, Yarkevich A.1, Ragulin V.1
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Учреждения:
- Institute of Physiologically Active Substances
- Выпуск: Том 87, № 12 (2017)
- Страницы: 2898-2901
- Раздел: Letters to the Editor
- URL: https://journals.rcsi.science/1070-3632/article/view/221731
- DOI: https://doi.org/10.1134/S107036321712026X
- ID: 221731
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Аннотация
A method for the synthesis of N-Cbz-protected phosphorylic analogs of proline by cyclic amidoalkylation of various hydrophosphorylic compounds was developed. Combination of amide and carbonyl fragments in the 4-N-Cbz-aminobutyraldehyde molecule allows to realize the three-center two-component amide version of the Kabachnik–Fields reaction.
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Об авторах
A. Vinyukov
Institute of Physiologically Active Substances
Email: rvalery@dio.ru
Россия, Severnyi proezd 1, Chernogolovka, Moscow oblast, 142432
M. Dmitriev
Institute of Physiologically Active Substances
Email: rvalery@dio.ru
Россия, Severnyi proezd 1, Chernogolovka, Moscow oblast, 142432
A. Yarkevich
Institute of Physiologically Active Substances
Email: rvalery@dio.ru
Россия, Severnyi proezd 1, Chernogolovka, Moscow oblast, 142432
V. Ragulin
Institute of Physiologically Active Substances
Автор, ответственный за переписку.
Email: rvalery@dio.ru
Россия, Severnyi proezd 1, Chernogolovka, Moscow oblast, 142432
